Nonaka Aoi, Yamamoto Haruki, Kamiya Narumi, Kotani Hiroya, Yamakawa Hisanori, Tsujimoto Ryoma, Fujita Yuichi
School of Agricultural Sciences, Nagoya University, Nagoya, Japan.
Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan.
Front Microbiol. 2019 Mar 15;10:495. doi: 10.3389/fmicb.2019.00495. eCollection 2019.
Since nitrogenase is extremely vulnerable to oxygen, aerobic or micro-aerobic nitrogen-fixing organisms need to create anaerobic microenvironments in the cells for diazotrophic growth, which would be one of the major barriers to express active nitrogenase in plants in efforts to create nitrogen-fixing plants. Numerous cyanobacteria are able to fix nitrogen with nitrogenase by coping with the endogenous oxygen production by photosynthesis. Understanding of the molecular mechanisms enabling to the coexistence of nitrogen fixation and photosynthesis in nonheterocystous cyanobacteria could offer valuable insights for the transfer of nitrogen fixation capacity into plants. We previously identified the gene encoding the master regulator for the nitrogen fixation () gene cluster in the genome of a nonheterocystous cyanobacterium , in addition to initial characterization of the gene cluster. Here we isolated nine mutants, in which the and -related genes were individually knocked out in to investigate the individual functions of (1) accessory proteins (NifW, NifX/NafY, and NifZ) in the biosynthesis of nitrogenase metallocenters, (2) serine acetyltransferase (NifP) in cysteine supply for iron-sulfur clusters, (3) pyruvate formate lyase in anaerobic metabolism, and (4) NifT and HesAB proteins. , , and exhibited the most severe phenotype characterized by low nitrogenase activity (<10%) and loss of diazotrophic growth ability. The phenotypes of , , and suggested that the functions of the homologous proteins NifX and NafY partially overlap. exhibited significantly slower diazotrophic growth than the wild type, with lower nitrogenase activity (22%). The other four mutants (, , , and ) grew diazotrophically similar to the wild type. Western blot analysis revealed a high correlation between nitrogenase activity and NifD contents, suggesting that NifD is more susceptible to proteolytic degradation than NifK in . The phenotype of the mutants lacking the accessory proteins was more severe than that observed in heterotrophic bacteria such as , which suggests that the functions of NifW, NifX/NafY, and NifZ are critical for diazotrophic growth of oxygenic photosynthetic cells. provides a promising model for studying the molecular mechanisms that produce active nitrogenase, to facilitate the creation of nitrogen-fixing plants.
由于固氮酶对氧气极为敏感,需氧或微需氧的固氮生物需要在细胞内创造厌氧微环境以进行固氮生长,这将是在培育固氮植物的过程中在植物中表达活性固氮酶的主要障碍之一。许多蓝细菌能够通过应对光合作用产生的内源性氧气来利用固氮酶固定氮。了解非异形胞蓝细菌中使固氮作用与光合作用共存的分子机制可为将固氮能力转移到植物中提供有价值的见解。我们之前在一种非异形胞蓝细菌的基因组中鉴定出了编码固氮()基因簇主调控因子的基因,此外还对该基因簇进行了初步表征。在此,我们分离出了九个突变体,其中在中分别敲除了和相关基因,以研究(1)固氮酶金属中心生物合成中的辅助蛋白(NifW、NifX/NafY和NifZ)、(2)为铁硫簇提供半胱氨酸的丝氨酸乙酰转移酶(NifP)、(3)厌氧代谢中的丙酮酸甲酸裂解酶以及(4)NifT和HesAB蛋白的各自功能。、和表现出最严重的表型,其特征为固氮酶活性低(<10%)且丧失固氮生长能力。、和的表型表明同源蛋白NifX和NafY的功能部分重叠。表现出比野生型明显更慢的固氮生长速度,固氮酶活性较低(22%)。其他四个突变体(、、和)的固氮生长情况与野生型相似。蛋白质免疫印迹分析显示固氮酶活性与NifD含量高度相关,这表明在中NifD比NifK更容易受到蛋白水解降解。缺乏辅助蛋白的突变体的表型比在诸如等异养细菌中观察到的更严重,这表明NifW、NifX/NafY和NifZ的功能对于光合细胞的固氮生长至关重要。为研究产生活性固氮酶的分子机制提供了一个有前景的模型,以促进固氮植物的培育。